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Clinical Trials/NCT04555005
NCT04555005CompletedNot Applicable

Implementation of a Mindfulness-based Crisis Intervention for Frontline Healthcare Workers During the COVID-19 Outbreak in a Public General Hospital in Madrid, Spain

Instituto de Investigación Hospital Universitario La Paz2 sites in 1 country1,000 target enrollmentStarted: March 10, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,000
Locations
2
Primary Endpoint
Perceived helpfulness to reduce current stress

Study Overview

Brief Summary

The COVID-19 outbreak is having an impact on the well-being of healthcare workers. Previous reports on pandemics show that such an impact may last beyond the time of the outbreak. Mindfulness-based interventions help healthcare professionals to reduce stress and may foster resilience and recovery, although they have never been tested in a context such as the current one. This single-arm trial explores the acceptability, safety and usefulness of an on-site, brief Mindfulness-based intervention to reduce stress for front line health workers during a crisis.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • All frontline healthcare workers present in the ward at the time of intervention

Exclusion Criteria

  • Extreme adverse events

Arms & Interventions

Mindfulness based intervention

Other

Mindfulness based intervention for frontline healthcare workers during COVID-19 outbreak

Intervention: Mindfulness based intervention (Other)

Outcomes

Primary Outcomes

Perceived helpfulness to reduce current stress

Time Frame: through study completion, up to three days

The outcome was measured by a 10-point visual analogue scale developed for this study, where 0 was "it did not help me at all" and 10 was "it helped me a lot".

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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